meddevicedb.com FDA Device Reference

GUTTA GUN

K771406 Class I Traditional
Decision Date
1977-08-26
Sponsor / Applicant
Aus-Tex Dental Mfg. & Design

Technical Specification

510(k) Submission ID K771406
Product Code EIC
Medical Specialty / Panel Dental
Regulation Citation 21 CFR 872.4565
Decision Date 1977-08-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

GUTTA GUN received FDA 510(k) clearance under submission number K771406, sponsored by Aus-Tex Dental Mfg. & Design. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 1977-08-26.

Classification & Regulation

This clearance is catalogued under FDA product code EIC and 21 CFR 872.4565, within the Dental review panel as a Class I device.